Mutagenetix > Incidental Mutation

Incidental Mutation 'R5895:Or4x13'

457432

Institutional Source

Beutler Lab

Gene Symbol

Or4x13

Ensembl Gene

ENSMUSG00000082980

Gene Name

olfactory receptor family 4 subfamily X member 13

Synonyms

Olfr1274-ps, MOR228-5, MOR228-4, GA_x6K02T2Q125-51676372-51677301, Olfr1274

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.096) question?

Stock #

R5895 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

90230984-90232018 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 90231800 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 265 (I265T)

Ref Sequence

ENSEMBL: ENSMUSP00000148849 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000120681] [ENSMUST00000216111]

AlphaFold

A0A1L1SQ02

Predicted Effect

probably benign
Transcript: ENSMUST00000120681
AA Change: I265T

PolyPhen 2 Score 0.275 (Sensitivity: 0.91; Specificity: 0.88)

Predicted Effect

probably benign
Transcript: ENSMUST00000216111
AA Change: I265T

PolyPhen 2 Score 0.275 (Sensitivity: 0.91; Specificity: 0.88)

Coding Region Coverage

1x: 99.9%
3x: 99.4%
10x: 97.3%
20x: 91.7%

Validation Efficiency

98% (64/65)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb1a	G	A	5: 8,752,216 (GRCm39)	G426S	probably damaging	Het
Casp4	A	T	9: 5,328,573 (GRCm39)		probably benign	Het
Ccdc40	T	A	11: 119,144,229 (GRCm39)	F988Y	probably damaging	Het
Ccdc9b	T	C	2: 118,590,098 (GRCm39)	T249A	probably benign	Het
Chd5	T	A	4: 152,464,389 (GRCm39)	V1516E	probably benign	Het
Chrnd	T	A	1: 87,123,389 (GRCm39)		probably null	Het
Col5a3	C	A	9: 20,683,738 (GRCm39)	G1506V	unknown	Het
Csgalnact2	A	T	6: 118,106,215 (GRCm39)	C34*	probably null	Het
Ddx23	T	C	15: 98,549,832 (GRCm39)	K195E	probably benign	Het
Dhps	T	G	8: 85,800,880 (GRCm39)	S240A	probably benign	Het
Dnah5	T	A	15: 28,234,599 (GRCm39)		probably null	Het
Dock10	T	C	1: 80,514,676 (GRCm39)	T1414A	probably benign	Het
Dock4	A	G	12: 40,805,812 (GRCm39)	D928G	probably damaging	Het
Dolpp1	T	C	2: 30,285,658 (GRCm39)		probably benign	Het
Dse	T	A	10: 34,028,601 (GRCm39)	I830F	probably damaging	Het
Elmod1	C	T	9: 53,843,091 (GRCm39)	R29Q	probably damaging	Het
Ephx4	T	A	5: 107,577,518 (GRCm39)		probably null	Het
Evi5	A	T	5: 107,968,302 (GRCm39)	M215K	probably damaging	Het
Fbxl4	T	C	4: 22,390,678 (GRCm39)	L287P	probably damaging	Het
Gbp9	G	A	5: 105,230,724 (GRCm39)	S400L	probably damaging	Het
Gm6291	T	C	18: 6,371,365 (GRCm39)		noncoding transcript	Het
Gmcl1	A	T	6: 86,688,596 (GRCm39)	D301E	probably benign	Het
Gna14	C	T	19: 16,580,692 (GRCm39)	R177C	possibly damaging	Het
Golph3	C	T	15: 12,339,756 (GRCm39)	R90C	probably damaging	Het
Gpr142	T	A	11: 114,689,785 (GRCm39)	C12*	probably null	Het
Hat1	T	A	2: 71,239,357 (GRCm39)	N43K	possibly damaging	Het
Hivep1	A	T	13: 42,310,694 (GRCm39)	E978V	possibly damaging	Het
Hormad1	G	A	3: 95,467,044 (GRCm39)		probably null	Het
Kalrn	C	T	16: 33,795,805 (GRCm39)		probably benign	Het
Mars1	T	C	10: 127,132,418 (GRCm39)	T860A	probably benign	Het
Mdn1	A	T	4: 32,695,400 (GRCm39)	L1146F	probably damaging	Het
Met	A	G	6: 17,531,581 (GRCm39)	T620A	probably benign	Het
Mppe1	T	C	18: 67,358,834 (GRCm39)	E378G	probably benign	Het
Mybpc3	T	A	2: 90,955,010 (GRCm39)	V481D	probably damaging	Het
Myh14	A	T	7: 44,256,133 (GRCm39)	L1924Q	probably damaging	Het
Mylip	G	T	13: 45,562,178 (GRCm39)	E327*	probably null	Het
Naip1	C	T	13: 100,559,636 (GRCm39)	G1123R	probably benign	Het
Naip6	A	G	13: 100,452,500 (GRCm39)	V187A	possibly damaging	Het
Ncam1	T	A	9: 49,418,343 (GRCm39)	T986S	probably benign	Het
Or13p4	T	C	4: 118,547,314 (GRCm39)	I112V	probably damaging	Het
Phactr2	C	T	10: 13,121,261 (GRCm39)	G480S	probably damaging	Het
Por	A	G	5: 135,744,838 (GRCm39)	I34V	probably benign	Het
Ppp2r5b	C	T	19: 6,284,764 (GRCm39)	R33H	probably damaging	Het
Prkdc	C	A	16: 15,570,693 (GRCm39)	Y2325*	probably null	Het
Prx	A	G	7: 27,214,709 (GRCm39)	E73G	probably damaging	Het
Rbms2	C	A	10: 127,981,556 (GRCm39)	A126S	possibly damaging	Het
Rhoq	C	T	17: 87,302,117 (GRCm39)	A111V	probably damaging	Het
Rpl14	T	A	9: 120,403,240 (GRCm39)		probably benign	Het
Serbp1	A	G	6: 67,249,870 (GRCm39)	*75W	probably null	Het
Sptbn1	C	A	11: 30,073,978 (GRCm39)	V1351F	probably damaging	Het
Supt16	A	G	14: 52,401,979 (GRCm39)	V897A	probably benign	Het
Tfdp1	T	A	8: 13,407,038 (GRCm39)		probably null	Het
Ttn	T	A	2: 76,780,487 (GRCm39)	Y1088F	probably damaging	Het
Vmn2r105	G	T	17: 20,448,929 (GRCm39)	Q83K	probably benign	Het
Wdr76	A	T	2: 121,359,323 (GRCm39)	S221C	probably damaging	Het
Zfhx2	G	T	14: 55,303,348 (GRCm39)	F1545L	probably benign	Het
Zfp318	A	G	17: 46,709,959 (GRCm39)	I561V	probably damaging	Het

Other mutations in Or4x13

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R4073:Or4x13	UTSW	2	90,231,337 (GRCm39)	missense	probably benign	0.34
R4812:Or4x13	UTSW	2	90,231,440 (GRCm39)	missense	probably benign	0.04
R4989:Or4x13	UTSW	2	90,231,107 (GRCm39)	missense	probably benign	0.11
R5134:Or4x13	UTSW	2	90,231,107 (GRCm39)	missense	probably benign	0.11
R7419:Or4x13	UTSW	2	90,231,803 (GRCm39)	missense	probably damaging	1.00
R7585:Or4x13	UTSW	2	90,231,367 (GRCm39)	missense	probably damaging	1.00
R7957:Or4x13	UTSW	2	90,231,395 (GRCm39)	missense	probably damaging	1.00
R8334:Or4x13	UTSW	2	90,231,277 (GRCm39)	missense	probably benign	0.04
R9192:Or4x13	UTSW	2	90,231,716 (GRCm39)	missense	probably damaging	1.00
R9295:Or4x13	UTSW	2	90,231,441 (GRCm39)	missense	probably benign
R9313:Or4x13	UTSW	2	90,231,917 (GRCm39)	missense	probably benign	0.05
R9649:Or4x13	UTSW	2	90,231,338 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGATCAGCTTTGTGGTCCTC -3'
(R):5'- GGTGGACGATACAGAACTCTC -3'

Sequencing Primer
(F):5'- GTGGTCCTCTTATCATCCTATGCAG -3'
(R):5'- AACTCACTTTGTAGATCAGGCTGG -3'

Posted On

2017-02-15